KANSL1, KAT8 regulatory NSL complex subunit 1, 284058

N. diseases: 140; N. variants: 332
Disease: Parkinson Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7521
rs7521
Entrez Id: 4137;284058
Gene Symbol: MAPT;KANSL1
MAPT;KANSL1
CUI: C0030567
Disease:
Parkinson Disease 		0.010 GeneticVariation BEFREE This observation highlights the significance of rs7521 in modifying the age at onset of PD under a common haplotype background. 19450659 2009